-
Invariant patterns of clonal succession determine specific clinical features of Myelodysplastic syndromes (MDS)
Study
phs001898
-
Myocardial Infarction Genetics Exome Sequencing Consortium: Registre Gironi del Cor
Study
phs000902
-
Prospective Procurement of Solid Tumor Tissue to Identify Novel Therapeutic Targets
Study
phs001003
-
Genome Sequencing of Familial Cholangiocarcinoma for the Identification of Germline Risk Alleles
Study
phs001593
-
Genetics and Pathophysiology of Autoinflammatory Disorders
Study
phs001860
-
Multiregional Single-Cell Transcriptomic Analysis of Liver Cancer
Study
phs003117
-
NHLBI TOPMed: Pathways to Immunologically Mediated Asthma (PIMA)
Study
phs001727
-
High-Fidelity, Large-Scale Targeted Profiling of Microsatellites
Study
phs003679
-
Genetic Evaluation of Autoinflammatory Diseases
Study
phs001946
-
scRNA-seq of CD4+ T cells from blood and tumor of NSCLC patients
Study
EGAS50000000293
-
HGG panel sequencing
Study
EGAS50000000221
-
Transcriptome Sequencing PPGL (2)
Study
EGAS50000000013
-
Raw sequencing data from chromosome conformation capture, RNA sequencing and chromatin assays in human primary monocytes
Dataset
EGAD50000001116
-
EuroTARGET is a European study on mRCC, collecting clinical data, germline DNA, and tumor samples.
Study
EGAS50000000798
-
Synthetic - GDI synthetic data
Study
EGAS50000000678
-
Skin Microbiome of Monogenic Skin Disorder
Study
phs003799
-
Comparison Across Multiple Types of Sleep Deprivation
Study
phs003924
-
Genomic profiling of fragile X syndrome unmethylated full mutation carriers
Study
EGAS50000000648
-
Bulk RNAseq from in vitro generated macrophages and T cells, and mUM tumour biopsies
Dac
EGAC50000000518
-
The Heterogeneity Study of HeLa S3 Cells Based on Full-Length Single-Cell RNA-Seq
Study
phs001029
-
Spatial omics analysis of non-small cell lung cancers for revealing molecular statuses of intratumor heterogeneity and tumor microenvironment
Study
JGAS000613
-
A prospective trial comparing adaptive long-read sequencing and short-read genome sequencing for genetic diagnosis of cerebellar ataxia
Study
EGAS50000000573
-
Autoimmune-wide landscape of circulating CD4+ T cells unveils disease-specific heritability and phenotypic changes
Study
JGAS000578
-
Whole-exome sequencing of Helicobacter pylori-uninfected normal gastric gland
Study
JGAS000313
-
Research for drug discovery and elucidation of pathophysiology using disease-specific iPS cells
Study
JGAS000136
-
Identification of responsible genes and development of standardized medicine for familial breast cancer by genetic analysis with NGS technology
Study
JGAS000224
-
TMM whole genome analysis of 4566 Japanese individuals
Study
JGAS000239
-
Whole-exome sequencing of MDS and related myeloid neoplasms
Study
JGAS000023
-
Sarcopenia related to Head and Neck squamous cell carcinomas: transcriptome modifications of muscle cells induced by distant malignant cells
Study
EGAS50000000669
-
Genomic and epigenomic insights into the origin, pathogenesis and clinical behavior of mantle cell lymphoma subtypes
Study
EGAS00001004165
-
Intercellular nanotube-mediated mitochondrial transfer enhances T-cell metabolic fitness and antitumor efficacy
Study
EGAS00001007356
-
TRACERx 100: RNAseq data from the first 100 TRACERx tumours
Study
EGAS00001003458
-
Mutational_Signatures_of_relapse_in_rectal_cancer_FFPE_samples_in_the_CR07_clinical_trial
Study
EGAS00001000651
-
Exome_sequencing_of_a_cohort_of_Rett_syndromelike_patients
Study
EGAS00001002059
-
Sequencing of liver cancer cell lines
Study
EGAS00001002237
-
HipSci HumanHT 12 Expression BeadChip analysis - Usher syndrome and congenital eye defects
Study
EGAS00001002023
-
ESGI_Exome_sequencing_in_Circulating_Tumor_Cells_to_determine_therapy_related_markers_____
Study
EGAS00001000747
-
Mutational landscape of the transcriptome offers putative targets for immunotherapy of myeloproliferative neoplasms
Study
EGAS00001003486
-
Genomic study of an AT-AML
Study
EGAS00001004392
-
Immunogenomic landscape of hematological malignancies
Study
EGAS00001004444
-
APCDR AGV Project: The African Genome Variation Project(dense array genotyping data)
Study
EGAS00001000959
-
Carcinoma of the oral tongue (OTSCC) genomic landscape characterisation
Study
EGAS00001001329
-
Comprehensive molecular characterization of brainstem glioma
Study
EGAS00001004341
-
Dual-mTOR inhibitor Rapalink-1 reduces prostate cancer patient-derived xenograft growth and alters tumor heterogeneity
Study
EGAS00001004431
-
RRBS data from TRACERx non-small cell lung cancer (NSCLC) tumours and matched normal adjacent tissue.
Study
EGAS00001006523
-
FFPE, buffycoat and cell free DNA from N. German esophagus cancer patients - 2021
Study
EGAS00001006813
-
Pre-diagnostic saliva microbiota of Finnish children with autoimmune diseases
Study
EGAS00001006949
-
NEC
Study
EGAS00001007013
-
Combinatorial CRISPR screen identifies fitness effects of paralogues FAM50A and FAM50B
Dataset
EGAD00001006648
-
RNA sequencing data of in vitro differentiated megakaryocyte cells transduced with E527K and WT SRC
Dataset
EGAD00001008356